We have isolated and characterised microsatellite loci from Pelargonium sp.
to explore the potential of these markers for cultivar identification. Sma
ll-insert libraries from a zonal (Pelargonium x hortorum cv. Isabell) and a
n ivy-leaved variety (P. peltatum cv. Guenievre gergue) were enriched for d
(AG), d(AC), d(CAA), d(GAA) and d(GATA) repeats. Of 141 positive clones seq
uenced, 133 contained a microsatellite. Primers for PCR amplification were
designed to the flanking regions of 57 microsatellites, resulting in interp
retable amplification products of the expected size for 29 loci. Seventeen
primer pairs amplifying 18 loci were used to fingerprint 44 di- and tetra-p
loid Pelargonium accessions representative of commercially available variet
ies. Multilocus genotypes obtained at 3 loci distinguished among all access
ions, except for three known flower colour sports and a fourth, phenotypica
lly very similar, variety. Allelic composition was also identical within tw
o other sport 'families' typed at the same 18 loci. UPGMA and principal co-
ordinate analysis of pairwise distance matrices derived from PCR amplificat
ion patterns revealed four distinct assemblages. The first group consisted
of tetraploid P. x hortorum varieties, a second group contained diploid P.
x hortorum, a third, tetraploid P. peltatum accessions, while a fourth, ver
y distinct, group consisted solely of diploid P. peltatum varieties. Polymo
rphism in P. peltatum was equal or greater than in P. x hortorum at 17 of t
he 18 loci, indicating that the analysed P. peltatum varieties form a genet
ically more variable array.